Open rachanajain opened 1 year ago
Hi @rachanajain
the poorer-quality reads will have lower mapping rates, and also lower mapped length, and higher mismatch rates.
Thank you for your reply. Why do we expect mismatch rates to increase when the reads are identical except for base quality.
If you have two different FASTQ files, I am not sure I understand how their sequences can be identical. Lowe quality scores usually results in larger error rates.
What is the role of read quality in alignment. If say I have 2 sets of fastqs. One of them has reads that are 100bp long and have high quality scores. And another has identical sequences but the sequencing quality is poor, should I expect to see a difference in alignment rates ?